NDC codes

FDA NDC Directory
Product NDC (as listed)51393-5001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51393-5001Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
51393-5001-151393500101513935001011 BOTTLE, DISPENSING in 1 CARTON (51393-5001-1) / 10 mL in 1 BOTTLE, DISPENSINGMarketed from Feb 1, 2019
51393-5001-351393500103513935001031 BOTTLE, DISPENSING in 1 CARTON (51393-5001-3) / 30 mL in 1 BOTTLE, DISPENSINGMarketed from Oct 15, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Allergy Maximum StrengthSuffix: Maximum Strength
Generic name (nonproprietary)
urtica dioica, althaea officinalis root, inula helenium root, angelica archangelica root, pine needle oil (pinus sylvestris), sodium chloride, and silicon dioxide
Active ingredients
Urtica dioica whole — 8 [hp_C]/100mLAlthaea officinalis root — 34 [hp_C]/100mLInula helenium root — 55 [hp_C]/100mLAngelica archangelica root — 89 [hp_C]/100mLPine needle oil (Pinus sylvestris) — 89 [hp_C]/100mLSodium chloride — 55 [hp_C]/100mLSilicon dioxide — 89 [hp_C]/100mL
Dosage form
Solution/ drops
Route
Sublingual
Labeler
Forces of NatureNDC labeler code 51393
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 51393-5001_4b453b93-21bd-b234-e063-6294a90afd0bSPL ID 4b453b93-21bd-b234-e063-6294a90afd0bSPL set ID 122ca23e-43f1-4e5c-afc2-1418b1717679UNII 710FLW4U46, TRW2FUF47H, E55SMD6DA8, DTN01M69SN, 5EXL5H740Y, 451W47IQ8X, ETJ7Z6XBU4

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N451393500101 followed by a unit qualifier and the quantity

Package 51393-5001-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses For the temporary relief of allergy and hay fever symptoms including: Sneezing Runny Nose Itchy Eyes, Nose, Throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51393-5001

What is NDC 51393-5001?
51393-5001 is the product NDC for Allergy Maximum Strength, Urtica dioica whole 8 [hp_C]/100mL + 6 more ingredients solution/ drops, listed with the FDA by Forces of Nature. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Allergy Maximum Strength (Urtica Dioica, Althaea Officinalis Root, Inula Helenium Root, Angelica Archangelica Root, Pine Needle Oil (Pinus Sylvestris), Sodium Chloride, and Silicon Dioxide).
What is the active ingredient?
Urtica dioica whole, Althaea officinalis root, Inula helenium root, Angelica archangelica root, Pine needle oil (Pinus sylvestris), Sodium chloride, Silicon dioxide.
Who is the labeler?
Forces of Nature, NDC labeler code 51393. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allergy Maximum Strength?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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